Hinrichsen H, Halabi A, Kirch W
I. Medical Department, Christian-Albrechts-Universität, Kiel, West Germany.
Clin Pharmacol Ther. 1990 Sep;48(3):302-8. doi: 10.1038/clpt.1990.153.
In a randomized, placebo-controlled, double-blind study, 10 healthy volunteers were treated orally once a day for 1 week each with placebo, 800 mg cimetidine, 300 mg ranitidine, and 40 mg famotidine. On the seventh treatment day, heart rate, blood pressure, systolic time intervals, and impedance cardiography were measured before the morning dose and at 2, 6, 12, and 24 hours after the morning dose. Heart rate and blood pressure were not markedly altered by any of the H2-receptor antagonists compared with the findings for placebo. Cimetidine and ranitidine did not markedly alter parameters of systolic time interval and impedance cardiography compared with placebo in contrast to famotidine, which significantly decreased stroke volume, cardiac output, and the Heather Index in impedance cardiography (p less than 0.05) and also significantly increased the ratio of the preejection period to the left ventricular ejection time in systolic time interval (p less than 0.05) 2 hours after the morning dose. Six hours after administration, most of these alterations could no longer be detected. The observed changes in hemodynamic parameters confirm that famotidine exerts negative effects on cardiac performance, whereas such influences could not be shown for cimetidine and ranitidine.
在一项随机、安慰剂对照、双盲研究中,10名健康志愿者分别接受安慰剂、800毫克西咪替丁、300毫克雷尼替丁和40毫克法莫替丁治疗,每日口服1次,各治疗1周。在治疗的第7天,于晨服药物前以及晨服药物后2、6、12和24小时测量心率、血压、收缩期时间间期和阻抗心动图。与安慰剂组的结果相比,任何一种H2受体拮抗剂均未使心率和血压发生明显改变。与安慰剂相比,西咪替丁和雷尼替丁未明显改变收缩期时间间期和阻抗心动图参数,而法莫替丁则显著降低了阻抗心动图中的每搏输出量、心输出量和希斯指数(p<0.05),并且在晨服药物后2小时还显著增加了收缩期时间间期中射血前期与左心室射血时间的比值(p<0.05)。给药6小时后,这些改变大多不再能被检测到。观察到的血流动力学参数变化证实,法莫替丁对心脏功能有负面影响,而西咪替丁和雷尼替丁则未表现出此类影响。